Eucalyptus Cuprum sulf. (Uriel Pharmacy Inc.)


Welcome to the PulseAid listing for the Eucalyptus Cuprum sulf. drug offered from Uriel Pharmacy Inc.. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: Uriel Pharmacy Inc.
NON-PROPRIETARY NAME: Eucalyptus Cuprum sulf.
SUBSTANCE NAME: EUCALYPTUS GUM; CUPRIC SULFATE
TYPE: HUMAN OTC DRUG
PHARMA CLASS:
ROUTE: ORAL
DOSAGE FORM: PELLET
MARKETING CATEGORY NAME: UNAPPROVED HOMEOPATHIC
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00


Eucalyptus Cuprum sulf. HUMAN OTC DRUG Details:

Item DescriptionEucalyptus Cuprum sulf. from Uriel Pharmacy Inc.
LABELER NAME: Uriel Pharmacy Inc.
DEA SCHEDULE:
ACTIVE STRENGTH: 1; 5([hp_X]/1; [hp_X]/1)
START MARKETING DATE: 2009-09-01
END MARKETING DATE: 0000-00-00
PRODUCT ID: 48951-4046_576d08c1-f2b2-569f-e053-2991aa0aa1f8
PRODUCT NDC: 48951-4046
APPLICATION NUMBER:

Other EUCALYPTUS GUM; CUPRIC SULFATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
Uriel Pharmacy Inc.Eucalyptus Cuprum sulfuricum Special Order